Konica Li 10 and 10A Laser Imager
FDA 510(k) K920769 · Konica Corp.
510(k) numberK920769
Submission
- Device name
- Konica Li 10 and 10A Laser Imager
- Applicant
- Konica Corp.
New York, NY, US - Received
- February 6, 1992
- Decision date
- May 6, 1992
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) statement available from FDA
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Questions and answers
When was Konica Li 10 and 10A Laser Imager cleared by the FDA?
Konica Li 10 and 10A Laser Imager (K920769) received a 510(k) decision of Substantially Equivalent on May 6, 1992, 90 days after the submission was received.
What is the product code of K920769?
The FDA product code is LMC – Camera, Multi Format, Radiological, a Class II (moderate risk) device regulated under 21 CFR 892.2040.